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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1995 2
1996 5
1997 1
1998 1
1999 1
2000 2
2001 1
2002 1
2003 2
2004 2
2005 6
2006 9
2007 3
2008 4
2009 8
2010 4
2011 12
2012 6
2013 8
2014 8
2015 7
2016 8
2017 6
2018 3
2019 3
2020 5
2021 6
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Similar articles for PMID: 23681356

109 results
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Page 1
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X).
Basehore MJ, Michaelson-Cohen R, Levy-Lahad E, Sismani C, Bird LM, Friez MJ, Walsh T, Abidi F, Holloway L, Skinner C, McGee S, Alexandrou A, Syrrou M, Patsalis PC, Raymond G, Wang T, Schwartz CE, King MC, Stevenson RE. Basehore MJ, et al. Clin Genet. 2015 May;87(5):461-6. doi: 10.1111/cge.12420. Epub 2014 May 30. Clin Genet. 2015. PMID: 24805811 Review.
Mutations in the chromatin-associated protein ATRX.
Gibbons RJ, Wada T, Fisher CA, Malik N, Mitson MJ, Steensma DP, Fryer A, Goudie DR, Krantz ID, Traeger-Synodinos J. Gibbons RJ, et al. Hum Mutat. 2008 Jun;29(6):796-802. doi: 10.1002/humu.20734. Hum Mutat. 2008. PMID: 18409179
Partial ATRX gene duplication causes ATR-X syndrome.
Cohn DM, Pagon RA, Hudgins L, Schwartz CE, Stevenson RE, Friez MJ. Cohn DM, et al. Am J Med Genet A. 2009 Oct;149A(10):2317-20. doi: 10.1002/ajmg.a.33006. Am J Med Genet A. 2009. PMID: 19764021 No abstract available.
Partial duplications of the ATRX gene cause the ATR-X syndrome.
Thienpont B, de Ravel T, Van Esch H, Van Schoubroeck D, Moerman P, Vermeesch JR, Fryns JP, Froyen G, Lacoste C, Badens C, Devriendt K. Thienpont B, et al. Eur J Hum Genet. 2007 Oct;15(10):1094-7. doi: 10.1038/sj.ejhg.5201878. Epub 2007 Jun 20. Eur J Hum Genet. 2007. PMID: 17579672
109 results
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